Long QT Syndrome:.
Author:
Publisher
Wiley
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8167.2000.tb00035.x/fullpdf
Reference6 articles.
1. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
2. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
3. Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
4. Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
5. Functional Effects of Mutations in KvLQT1 that Cause Long QT Syndrome
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2. Whole-exome sequencing and electrophysiological study reveal a novel loss-of-function mutation of KCNA10 in epinephrine provoked long QT syndrome with familial history of sudden cardiac death;Legal Medicine;2023-05
3. Association of the P441L KCNQ1 variant with severity of long QT syndrome and risk of cardiac events;Frontiers in Cardiovascular Medicine;2022-10-31
4. Mutation location and IKs regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region;European Heart Journal;2021-09-10
5. Clinical Advances in Congenital Long QT Syndrome;Cardiology Discovery;2021-04-08
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